Evolution of platelet functions in cirrhotic patients undergoing liver transplantation: A prospective exploration over a month.
Daniel EyraudLudovic SunerAxelle DupontChristilla Bachelot-LozaDavid M SmadjaDominique HelleySébastien BertilOvidiu GostianJean SzymezakYann LoncarLouis PuybassetPascal LebrayCorinne VezinetJean-Christophe VaillantBenjamin GrangerPascale GaussemPublished in: PloS one (2018)
This prospective observational study was designed to analyze platelet functions across time in 50 patients scheduled for liver transplantation (LT) secondary to decompensated cirrhosis or hepatocellular carcinoma. Platelet functions were assessed before LT (pre-LT), one week (D7) and 1 month (D28) after LT. Platelet count significantly increased from pre-LT time to day 28 as well as circulating CD34+hematopoietic stem cells. To avoid any influence of platelet count on assays, platelet function was evaluated on platelet-rich-plasma adjusted to pre-LT platelet count. Although platelet secretion potential did not differ between time-points, as evaluated by the expression of CD62P upon strong activation, platelet aggregation in response to various agonists significantly increased along time, however with no concomitant increase of circulating markers of platelet activation: platelet microvesicles, platelet-leukocyte complexes, soluble CD40L and soluble CD62P. In the multivariate analysis, hepatic function was associated with platelet count and function. A lower platelet aggregation recovery was correlated with Child C score. History of thrombosis or bleeding was associated with respective higher or lower values of platelet aggregation. This longitudinal analysis of platelet functions in LT patients showed an improvement of platelet functions along time together with platelet count increase, with no evidence of platelet hyperactivation at any time-point.
Keyphrases
- stem cells
- end stage renal disease
- patients undergoing
- chronic kidney disease
- mesenchymal stem cells
- peripheral blood
- risk assessment
- poor prognosis
- newly diagnosed
- platelet rich plasma
- bone marrow
- atrial fibrillation
- hepatitis b virus
- peritoneal dialysis
- cross sectional
- binding protein
- patient reported outcomes
- long non coding rna
- study protocol